Variant report

Variant	rs67213527
Chromosome Location	chr13:84701445-84701446
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17077783	1.00[EUR][1000 genomes]
rs56742355	0.87[AMR][1000 genomes]
rs61318536	0.87[AMR][1000 genomes]
rs66697853	0.93[EUR][1000 genomes]
rs67896489	0.87[AMR][1000 genomes]
rs7324310	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9531555	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9531556	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9531557	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9531558	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9546612	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9546613	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9546614	0.98[EUR][1000 genomes]
rs9546615	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9546616	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9546618	0.98[EUR][1000 genomes]
rs9546621	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046982	chr13:84631965-84800765	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1038880	chr13:84632431-84861839	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv949402	chr13:84675752-85606846	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1035493	chr13:84683545-84779862	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv900687	chr13:84691001-84714655	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv562557	chr13:84695884-84714655	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:84700600-84701800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr13:84700600-84702000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr13:84700800-84701600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr13:84700800-84701600	Enhancers	Esophagus	oesophagus
5	chr13:84700800-84701600	Enhancers	NHEK	skin
6	chr13:84700800-84701800	Enhancers	Primary T cells fromperipheralblood	blood
7	chr13:84701000-84701800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr13:84701200-84701600	Enhancers	Fetal Heart	heart

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links